A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932003



Internal ID22707295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42467487..42468721hg38UCSC Ensembl
chr15:42759685..42760919hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385281
Samples
Known GenesZNF106
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932003
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer